Multiple aspects of amyloid dynamics in vivo integrate to establish prion variant dominance in yeast

Prion variants are self-perpetuating conformers of a single protein that assemble into amyloid fibers and confer unique phenotypic states. Multiple prion variants can arise, particularly in response to changing environments, and interact within an organism. These interactions are often competitive, with one variant establishing phenotypic dominance over the others. This dominance has been linked to the competition for non-prion state protein, which must be converted to the prion state via a nucleated polymerization mechanism. However, the intrinsic rates of conversion, determined by the conformation of the variant, cannot explain prion variant dominance, suggesting a more complex interaction. Using the yeast prion system [PSI+], we have determined the mechanism of dominance of the [PSI+]Strong variant over the [PSI+]Weak variant in vivo. When mixed by mating, phenotypic dominance is established in zygotes, but the two variants persist and co-exist in the lineage descended from this cell. [PSI+]Strong propagons, the heritable unit, are amplified at the expense of [PSI+]Weak propagons, through the efficient conversion of soluble Sup35 protein, as revealed by fluorescence photobleaching experiments employing variant-specific mutants of Sup35. This competition, however, is highly sensitive to the fragmentation of [PSI+]Strong amyloid fibers, with even transient inhibition of the fragmentation catalyst Hsp104 promoting amplification of [PSI+]Weak propagons. Reducing the number of [PSI+]Strong propagons prior to mating, similarly promotes [PSI+]Weak amplification and conversion of soluble Sup35, indicating that template number and conversion efficiency combine to determine dominance. Thus, prion variant dominance is not an absolute hierarchy but rather an outcome arising from the dynamic interplay between unique protein conformations and their interactions with distinct cellular proteostatic niches.


Introduction
Prions are proteins capable of transmitting novel physiological states, either vertically or horizontally, among individuals.In mammals, the archetype is the prion protein PrP, which is the infectious agent in the transmissible spongiform encephalopathies (TSEs), including Cruetzfeldt-Jakob's disease (CJD) in humans, scrapie in sheep and goats, chronic Norton et al. 10.3389/fnmol.2024.1439442Frontiers in Molecular Neuroscience 02 frontiersin.orgwasting disease (CWD) in cervids, and bovine spongiform encephalopathy (BSE, also known as 'mad-cow disease') in cattle (McKinley et al., 1983;Kitamoto et al., 1986;Allsop et al., 1988;Hope et al., 1988;Borchelt et al., 1990;Caughey and Raymond, 1991;Bartz et al., 1998;Collinge, 2001).Prions have also been identified in fungi such as S. cerevisiae and P. anserina and are associated with the modulation of a wide range of cellular pathways including nitrogen metabolism and translation termination (Wickner, 2016).While these states are not considered to be pathogenic, they often alter the adaptive advantage of the organism (Tuite and Serio, 2010;Wickner, 2016).In all known systems, prion-associated physiological states are self-perpetuating, operationally expanding the function of genetic determination to proteins (Serio and Lindquist, 1999).
The engendering of genetic functions in prion proteins results directly from their conformational flexibility.These proteins can adopt alternative folds beyond their native structures that are rich in β-sheets.These secondary structures stack laterally through backbone hydrogen bonding to facilitate oligomerization and the formation of fibrillary structures known as amyloids (Pan et al., 1993;Chiti and Dobson, 2006;Wickner et al., 2008;Knowles et al., 2014), which also self-associate to form higher-order assemblies (Naeimi and Serio, 2022).Amyloidogenicity is frequently associated with intrinsically disordered regions of these proteins (Chiti and Dobson, 2016), resulting in a suite of amyloid structures for each protein (Diaz-Avalos et al., 2005;Nelson et al., 2005;Toyama et al., 2007).These quaternary structures are associated with distinct and transmissible biological outcomes, impacting the stability, severity, sequelae, incubation time, tropism, and interspecies transmissibility of the prion physiological state (Bessen and Marsh, 1994;Tanaka et al., 2006;Makarava et al., 2009;Terry et al., 2016).Together these structural and biological characteristics define unique prion variants, also known as strains, in mammals and fungi.
The variant-specific amyloid structures are defined by a core of distinct self-interactions among monomers of the same protein, which in turn determine the kinetic and thermodynamic stability of the complex and the minimum size of the assembly competent nucleation seed (Chiti et al., 2003;Knowles et al., 2014;Villali et al., 2020).These parameters connect the amyloid structure to its physiological impacts through an integrated system known as the nucleated polymerization model (NPM) (Nowak et al., 1998;Masel et al., 1999), which also captures the behavior of non-infectious amyloids such as α-synuclein in Parkinson's Disease and Multiple System Atrophy (MSA) and Aβ and tau in Alzheimer's disease, among others (Jucker and Walker, 2013;Walker et al., 2013).Specifically, each amyloid structure can be uniquely defined by three parameters: (1) the rate of conformational conversion of the non-prion conformer through association at and incorporation onto the fiber ends, (2) the rate of fragmentation of growing fibers to generate new templating surfaces, and the (3) the size-based persistence of individual aggregates arising from these dynamics (Masel et al., 1999;Tanaka et al., 2006;Villali et al., 2020).Together, these processes determine the variant-specific ratio of protein in the prion and non-prion states and the size distribution of amyloid aggregates in vivo.As a result, the degree of functional alteration of the protein is established and manifests as different "strengths" of the prion physiological state (Masel et al., 1999;Tanaka et al., 2006;Pezza et al., 2014).The transmissibility of the amyloid is also impacted by its size, contributing to the stability of the physiological state (Silveira et al., 2005;Derdowski et al., 2010).
Beyond existing as individual isolates, prion variants can co-exist within the same host.These mixtures may arise spontaneously (Collinge and Clarke, 2007;Bateman and Wickner, 2013).Evidence also suggests that existing variants can interchange, known as evolution, adaptation, or "mutation, " under selective pressure upon passage through a different host (Bruce and Dickinson, 1987;Santoso et al., 2000) or genetic background (Doel et al., 1994;Derkatch et al., 1999;DiSalvo et al., 2011;Lin et al., 2011;Yu and King, 2018) or in the presence of small molecules or pharmacological agents (Ghaemmaghami et al., 2009;Roberts et al., 2009;Shorter, 2010;Oelschlegel and Weissmann, 2013).At the phenotypic level, individual variants have been reported to establish dominance in mixtures, with the characteristics of the mixture typically being indistinguishable from those of the dominant variant (Tuite and Serio, 2010).Nonetheless, variant mixtures may also exhibit characteristics that are distinct from their isolated states (Kimberlin and Walker, 1978;Bessen and Marsh, 1992;Cali et al., 2009;Parchi et al., 2009).Thus, the interplay among prion variants is a crucial factor in understanding their physiological outcomes.
Studies of both mammalian and yeast prions suggest this interplay hinges on the relative rates of propagation of the interacting variants (Dickinson et al., 1972;Bradley et al., 2002;Tanaka et al., 2006).In the case of mammals, these differences have been shown to drive the competition for soluble prion protein, demonstrated in vitro in the presence of cellular cofactors using protein misfolding cyclic amplification (PMCA) (Atarashi et al., 2006(Atarashi et al., , 2007;;Bartz et al., 2007;Shikiya et al., 2010;Burke et al., 2020;Shikiya and Bartz, 2023).However, differences in the rate of conversion of non-prion state protein at the fiber ends cannot fully explain variant competition.Indeed, for the yeast prion [PSI + ], the amyloid form of the Sup35 protein, the [PSI + ] Weak variant is recessive to the [PSI + ] Strong variant despite having a higher intrinsic rate of conformational conversion (Bradley et al., 2002;Tanaka et al., 2006).According to the NPM, the number of templates available also contributes to the rate of propagation (Nowak et al., 1998), and, consistent with this idea, variant competition is impacted by the interval between inoculations and by the relative titer of each variant in mammals and by the number of transmissible templates known as propagons in yeast (Dickinson et al., 1972;Dickinson and Outram, 1979;Manuelidis, 1998;Bartz et al., 2000Bartz et al., , 2007;;Cox et al., 2003;Manuelidis and Lu, 2003;Tanaka et al., 2006;Schutt and Bartz, 2008;Shikiya et al., 2010;Lin et al., 2011;Diaz-Espinoza et al., 2018;Shikiya and Bartz, 2023).
In yeast, the amplification of amyloid templates has been directly linked to the AAA+ ATPase Hsp104, which fragments amyloid fibers along with its co-chaperones Hsp70 (i.e., Ssa1/2), Hsp110 (i.e., Sse1/2) and Hsp40 (i.e., Sis1) (Chernoff et al., 1995;Song et al., 2005;Satpute-Krishnan et al., 2007;Higurashi et al., 2008;Sadlish et al., 2008;Tipton et al., 2008).A similar amyloid-fragmenting activity has been linked to the Hsp110, Hsp70, Hsp40 system in mammals (Gao et al., 2015).While factors other than the prion protein itself are involved in the formation of prion templates, the influence of this pathway on prion variant competition is mechanistically unexplored.Here, we assess this possibility using the yeast prion [PSI + ], as a model system.We find that the [PSI + ] Strong and [PSI + ] Weak variants co-exist in vivo when introduced into the same cell by mating and compete directly for soluble Sup35 protein in the non-prion state.This competition is sensitive to the activity of Hsp104, which is necessary to amplify [PSI + ] Strong templates to a level capable of overcoming the higher rate of conversion of the [PSI + ] Weak variant.Thus, the integration of intrinsic and extrinsic forces shapes prion variant interactions.

Prion variant dominance is established immediately upon mating
When [PSI + ] Strong and [PSI + ] Weak variants are introduced into the same cytoplasm by mating, the [PSI + ] Strong phenotype usually dominates at the colony level, following ~20 generations of growth (Derkatch et al., 1996;King, 2001;Bradley et al., 2002).However, it is unclear when or how this dominance is established.To examine prion variant competition in yeast, we first determined the temporal appearance of the [PSI + ] Strong phenotype during competition initiated by mating yeast haploids propagating different prion states and variants.
The [PSI + ] prion-associated phenotype can be monitored at the colony level in strains with the ade1-14 genotype, which encodes a premature stop codon in the ADE1 open reading frame (Chernoff et al., 1995;Fitzpatrick et al., 2011).These strains can only grow in the absence of exogenous adenine if the premature stop codon is readthrough efficiently as occurs in [PSI + ] Strong but not [PSI + ] Weak or non-prion [psi − ] strains (Chernoff et al., 1995;Derkatch et al., 1996).To remove the interference of existing Ade1 protein in the crosses, we used one haploid that is disrupted for ADE1 (Δade1) in each cross, with the ade1-14 allele encoded in the other mating partner.As expected, zygotes resulting from mating an ade1-14 [psi − ] haploid and an Δade1 [psi − ] or [PSI + ] Weak haploid divide only a few times when transferred to medium lacking adenine (Figure 1A, dark and light gray, respectively); however, zygotes resulting from mating an ade1-14 [psi − ] haploid and an Δade1 [PSI + ] Strong haploid divide robustly in the absence of adenine (Figure 1A, white).Because the ade1-14 reporter only encounters the [PSI + ] Strong state upon mating, the prion-associated readthrough phenotype must be established in the zygote.
To determine whether the [PSI + ] Strong phenotype is established on the same timescale upon mating [PSI + ] Strong and [PSI + ] Weak haploids, we also created [PSI + ] Strong (Figure 1A, white) and [PSI + ] Weak (Figure 1A, light gray) strains with ADE1 disruptions.Zygotes formed by mating these haploids with an ade1-14 [psi − ] haploid divide similarly to those formed by mating them with an ade1-14 haploid propagating the same prion variant (i.e., mating two [PSI + ] Strong or two [PSI + ] Weak haploids; Figure 1A).In these crosses, the [PSI + ] Strong zygotes divide more robustly than the [PSI + ] Weak zygotes in the absence of adenine as expected.Thus, the prion-associated phenotypes of [PSI + ] Strong and [PSI + ] Weak are preserved in this experimental system.Zygotes formed by mating an ade1-14 [PSI + ] Weak haploid and an Δade1 [PSI + ] Strong haploid divide robustly in the absence of adenine and indistinguishably from a zygote formed by mating ade1-14 and Δade1 [PSI + ] Strong haploids together (Figure 1A, white), indicating a similar phenotype.Because the ade1-14 [PSI + ] Weak haploid is unable to divide robustly in the absence of adenine when mated to either an Δade1 [psi − ] or an [PSI + ] Weak haploid (Figure 1A, dark and light gray, respectively), our observations indicate that the [PSI + ] Strong variant establishes phenotypic dominance over the [PSI + ] Weak variant in the zygote.
As an alternative and more sensitive approach to assess the emergence of the [PSI + ] Strong phenotype in zygotes, we directly monitored stop codon readthrough efficiency using a YFP-based fluorescent reporter [i.e., GST(UGA)-YFP-NLS], whose nuclear expression requires the readthrough of a stop codon (Langlois et al., 2016).Zygotes formed by mating a [psi − ] haploid expressing the reporter to [psi − ], [PSI + ] Weak , or [PSI + ] Strong haploids exhibit increasing nuclear fluorescence intensities, respectively (Supplementary Figure S1).Thus, the reporter captures the phenotypic differences in the efficiency of stop codon readthrough expected of these strains (Derkatch et al., 1996).We next expressed the reporter in a [PSI + ] Weak haploid and performed the same crosses.Upon mating to a [psi − ] haploid, weak fluorescence is observed in the zygote.This baseline level of fluorescence increases in zygotes formed by mating a [PSI + ] Weak haploid expressing the reporter to a [PSI + ] Weak and to a [PSI + ] Strong haploid (Figures 1B,C).Because this level of stop codon readthrough exceeds that observed in the zygotes formed by mating the reporter haploid to a [psi − ] haploid (Figures 1B,C), [PSI + ] Strong has established phenotypic dominance in the zygote.

[PSI + ] Strong phenotypic dominance is established without elimination of [PSI + ] Weak aggregates
The [PSI + ] Strong variant may establish phenotypic dominance by eliminating Sup35 aggregates of the [PSI + ] Weak variant or through other changes in Sup35 biogenesis.To directly assess whether Sup35 aggregates of the [PSI + ] Weak variant persist in zygotes after mating [PSI + ] Strong and [PSI + ] Weak haploids, we quantified variant-specific heritable prion aggregates, known as propagons, in zygotes using an established plating assay (Cox et al., 2003) To determine whether Sup35 [PSI+]Weak aggregates persist as the zygote formed by mating [PSI + ] Strong and [PSI + ] Weak haploids divides to form a microcolony, we monitored their persistence using a GFP fusion to the G20D mutant of Sup35 (King, 2001), which forms fluorescent foci in [PSI + ] Weak but not in [PSI + ] Strong strains (Supplementary Figure S2A).As a control, we mated a [psi − ] haploid expressing a tetracycline-inducible copy of Sup35(G20D)-GFP to [psi − ], [PSI + ] Strong , and [PSI + ] Weak haploids and then induced expression of the GFP-tagged protein following the transfer of zygotes to medium containing doxycycline.In the resulting microcolonies, Sup35(G20D)-GFP remains diffuse when the reporter strain is mated to either [psi − ] (Supplementary Figure S2B) or [PSI + ] Strong haploids (Supplementary Figure S2C), but fluorescent foci are visible in some descendants of zygotes resulting from crosses to a [PSI + ] Weak haploid (Supplementary Figure S2D), demonstrating the specificity of this approach.

[PSI + ] Strong interferes with the amplification of [PSI + ] Weak propagons but not vice-versa
Given the persistence of Sup35 [PSI+]Weak aggregates in the presence of [PSI + ] Strong (Figure 2), prion variant competition likely arises through an alteration in the biogenesis of Sup35 in the presence of [PSI + ] Strong .To explore the potential targets of such an alteration, we first assessed propagon numbers in zygotes formed by mixing different prion states and variants.
In   S3. (B) The number of [PSI + ] Weak propagons from the zygotes presented in (A) was quantified and presented as box-whisker plots as in (A).The equality of means across all groups was tested using Welch's ANOVA test (p* ANOVA ); p-values were determined using pairwise unequal variance t-tests and are presented above each box plot for comparisons within a cross.The absence of a p-value for comparisons within a cross indicates a lack of significant difference.Full statistical comparisons are available in Supplementary Table S4.(C) The persistence of the [PSI + ] Weak variant was observed by microscopy in crosses between [PSI + ] Strong and [PSI + ] Weak haploids expressing Sup35(G20D)-GFP under the control of the P tetO7 promoter.GFP foci were detected in cells at the periphery of the resulting microcolony, indicated by white arrows in the inset (200-fold magnification).2A) propagons and is aligned with the phenotypic dominance of the latter (Figure 1), variant competition occurs at the level of amplification of the prion heritable unit.

[PSI + ] Strong outcompetes [PSI + ] Weak for conversion of Sup35 in vivo
Amplification of propagons requires conversion of soluble Sup35 to the prion state and fragmentation and transmission of prion aggregates; thus, competition could arise at either or both of these events.Both empirical data and mathematical models propose that conversion of soluble protein to the prion state is key to determining outcomes in prion variant competition (Tanaka et al., 2006;Shikiya et al., 2010).Given the phenotypic dominance of [PSI + ] Strong , we predict that soluble Sup35 will be more efficiently converted to the [PSI + ] Strong than the [PSI + ] Weak state in zygotes propagating both variants.To directly test this idea, we monitored Sup35-GFP transmissibility by fluorescence loss in photobleaching (FLIP), which we have previously demonstrated to be a sensitive assay of Sup35 physical state (Derdowski et al., 2010).
To determine the fate of Sup35 protein derived from a [PSI + ] Weak haploid in zygotes, we mated a [PSI + ] Weak haploid expressing Sup35-GFP to [PSI + ] Weak or [PSI + ] Strong haploids and monitored fluorescence loss in the dumbbell-shaped fused haploids during bleaching of the daughter bud.In matings between [PSI + ] Weak haploids, fluorescence is lost at a rate of 4.2 × 10 −3 s −1 (Figure 4A, salmon and Table 1).In matings between [PSI + ] Weak and [PSI + ] Strong haploids, fluorescence is lost at a rate of 2.3 × 10 −3 s −1 (Figure 4A, blue and Table 1).The reduced rate of fluorescence loss across the bud neck in the zygotes formed by mating [PSI + ] Strong and [PSI + ] Weak haploids is consistent with an increase in aggregated Sup35 relative to that found in zygotes formed by mating [PSI + ] Weak haploids alone.Because this decreased rate correlated with the amplification of [PSI + ] Strong propagons (Figure 2A), it likely represents the incorporation of soluble Sup35 into aggregates in the [PSI + ] Strong state.
If this prediction is accurate, the reduction in the rate of fluorescence loss in the presence of [PSI + ] Strong should not be observed in strains expressing Sup35(G20D)-GFP, which cannot be converted to the [PSI + ] Strong state (Supplementary Figure S2A) (King, 2001).To test this idea, we mated a [PSI + ] Weak haploid expressing Sup35(G20D)-GFP to [PSI + ] Weak and [PSI + ] Strong haploids.Fluorescence is lost at a rate of 2.9 × 10 −3 s −1 in the zygotes formed by mating the [PSI + ] Weak haploids alone and at a rate of 2.4 × 10 −3 s −1 in the zygotes formed by mating the [PSI + ] Strong and [PSI + ] Weak haploids (Figure 4B, salmon and blue, respectively, and Table 1), consistent with our prediction.Thus, the amplification of [PSI + ] Strong propagons and its phenotypic dominance in the presence of [PSI + ] Weak in zygotes are associated with the efficient incorporation of Sup35 into aggregates of the [PSI + ] Strong variant, providing direct evidence of competition at the protein level.

Amplification of [PSI + ] prion variants is differentially sensitive to Hsp104 activity
While our observations provide direct evidence of prion variant competition at the level of conversion of soluble Sup35 protein, the mechanism through which this competition arises remains unclear.For example, the preferential incorporation of Sup35 into aggregates of the [PSI + ] Strong variant in the presence of aggregates of the [PSI + ] Weak variant (Figure 4) cannot be explained by their biochemical properties, as the former catalyzes conversion at a lower rate than the latter in vitro (Tanaka et al., 2006).Thus, additional aspects of the in vivo prion cycle must impact variant competition.
Mathematical models of prion propagation indicate that the conversion of soluble protein is determined by the inherent rate of conversion by aggregates as well as by their number, which is tightly linked to the rate of fragmentation (Nowak et al., 1998;Masel et al., 1999).variant, we introduced a copy of Sup35 tagged with GFP that is expressed from the P MFA1 promoter.The P MFA1 promoter is a mating type a-specific promoter that is repressed upon mating (Galgoczy et al., 2004); thus, Sup35-GFP synthesis ceases, and the fate of the existing protein can be monitored over time (Satpute-Krishnan et al., 2007).Previously, we demonstrated that [PSI + ] Strong cells expressing Sup35-GFP from P MFA1 gradually lose their fluorescent foci due to fragmentation by Hsp104 and the incorporation of unlabeled Sup35, which continues to be synthesized (Satpute-Krishnan et al., 2007).However, if the fragmentation activity of Hsp104 is inhibited with guanidine HCl (GdnHCl) (Ferreira et al., 2001;Jung and Masison, 2001;Grimminger et al., 2004) While the fragmentation of Sup35 aggregates of the [PSI + ] Weak variant is not disadvantaged by the presence of the [PSI + ] Strong variant, fragmentation could still provide an advantage to the latter by promoting the observed amplification of propagons (Figure 2A).To  B).Thus, the amplification of [PSI + ] Strong propagons is more sensitive to the fragmentation activity of Hsp104 than that of [PSI + ] Weak propagons.

Template number drives prion variant competition in vivo
While the efficient incorporation of Sup35 protein (Figure 4 and Table 1) and the phenotypic dominance (Figure 1

Cross
Average (sec −1 ) 95% CI (sec −1 )    2A, 4), we hypothesized that [PSI + ] Weak more effectively competes with [PSI + ] Strong for Sup35 when propagon levels are more balanced.If this were the case, amplification of [PSI + ] Weak propagons is unlikely to be observed due to the incorporation of soluble Sup35 onto the larger aggregates present in a [PSI + ] Weak strain, which would have reduced transmission (Derdowski et al., 2010).Indeed, the amplification of [PSI + ] Weak propagons is significantly reduced in the presence of GdnHCl when a [PSI + ] Weak haploid is mated to a [psi − ] haploid but not to [PSI + ] Weak or [PSI + ] Strong haploids (Figure 3, compare white), the former of which contains high levels of soluble Sup35 as is the case for titrated [PSI + ] Strong (Supplementary Figure S3).
To test this idea, we monitored the fate of Sup35 protein by FLIP in zygotes formed by mating a titrated [PSI + ] Strong strain expressing Sup35-GFP to either a [PSI + ] Strong or [PSI + ] Weak strain.Fluorescence is lost at a rate of 4.4 × 10 −3 s −1 in the zygotes formed by mating titrated [PSI + ] Strong and [PSI + ] Strong haploids (Figure 6B, blue and Table 1), but the rate of fluorescence loss is more rapid (1.3 × 10 −2 s −1 ) when the same strain is mated to a [PSI + ] Weak haploid (Figure 6B, salmon and Table 1).These observations indicate that, when [PSI + ] Strong propagons are limiting, Sup35-GFP is more efficiently converted to the [PSI + ] state (i.e., slower rate of fluorescence loss) in the absence of the [PSI + ] Weak variant, consistent with the interference of [PSI + ] Weak in the amplification of [PSI + ] Strong propagons (Figure 2A).
If this interpretation is accurate, [PSI + ] Weak should not interfere with the conversion of a Sup35 mutant that can only adopt the [PSI + ] Strong state.To test this idea, we used the Sup35(11-61) fragment, which, when fluorescently tagged, forms foci in [PSI + ] Strong but not [PSI + ] Weak strains (Supplementary Figure S2) as previously suggested (King, 2001).We expressed Sup35(11-61)-GFP in the titrated [PSI + ] Strong strain and monitored its fate by FLIP in zygotes formed by mating to either [PSI + ] Strong or [PSI + ] Weak haploids.Fluorescence is lost at a rate of 9 × 10 −3 s −1 in zygotes formed by mating to a [PSI + ] Strong haploid and at a rate of 7.9 × 10 −3 s −1 in zygotes formed by mating to a [PSI + ] Weak haploid (Figure 6C, blue and salmon, respectively, and Table 1).The similar rates of fluorescence loss for the Sup35(11-61)-GFP protein in these two zygotes contrasts with the differential rates of fluorescence loss for wildtype Sup35-GFP in similar zygotes (Figure 6B and Table 1) and indicates that [PSI + ] Weak competes directly with [PSI + ] Strong for the conversion of Sup35 when propagons of the latter are limiting.

Discussion
Observations of interference among prion variants pre-date the prion hypothesis (Dickinson et al., 1972), but within this framework, the prevailing model links variant dominance to the competition for soluble prion protein (Bradley et al., 2002;Tanaka et al., 2006;Shikiya et al., 2010;Eckland et al., 2018).This conclusion is inferred from prion interference studies in vitro, using recombinant PrP C as the substrate in a simplified PMCA system (Atarashi et al., 2007).Here, our studies using the yeast [PSI + ] prion system provide direct in vivo evidence of variant competition for soluble Sup35 prion protein.Specifically, soluble Sup35 is efficiently converted to the dominant [PSI + ] Strong state in the presence of the recessive [PSI + ] Weak prion (Figure 4).This observation, while aligned with in vitro studies in mammals, cannot be explained by the intrinsic rate of conversion of the variants (Tanaka et al., 2006) nor can it account for transitions among prion variants from established mixtures, where dominance has already been established.However, our studies provide a new pathway for understanding these dynamics by probing early events following the mixing of prion variants in individual cells.When [PSI + ] Weak and [PSI + ] Strong variants are mixed in zygotes, the transmissible unit (i.e., the propagon) of the dominant [PSI + ] Strong variant is immediately amplified (Figure 2A), and this amplification is associated with an inhibition in amplification of propagons of the recessive [PSI + ] Weak variant (Figure 3).Within the context of the NPM, such amplification is based on rates of both conversion and fragmentation (Nowak et al., 1998;Masel et al., 1999).Previous studies have estimated the product of those rates to be higher for the dominant [PSI + ] Strong variant, despite its reduced rate of conversion at fiber ends, in comparison with the recessive [PSI + ] Weak variant (Tanaka et al., 2006), suggesting an enhanced dependence on fragmentation for the former.Indeed, transiently blocking the fragmentation activity of Hsp104 more significantly interferes with the amplification of [PSI + ] Strong than [PSI + ] Weak propagons in zygotes (Figures 2A,B); in contrast, the incorporation of soluble Sup35 more significantly interferes with the amplification of [PSI + ] Weak than [PSI + ] Strong propagons (Figures 2A,B).Together, these observations suggest, for the first time, that the interplay between both amyloid conversion and fragmentation are key factors in the competition among prion variants.
This expanded view of competition among prion variants provides a direct explanation for experimental manipulations known to alter the dominance of prion variants in mammals.Specifically, a recessive variant can effectively compete with a normally dominant variant if the former has increased titer or is inoculated in advance (Dickinson et al., 1972;Bartz et al., 2000).Presumably, the additional templates of the recessive variant resulting from these conditions are sufficient to overcome its relatively inefficient amplification, providing competitive advantage to the otherwise recessive variant.Indeed, the amplification of a recessive variant is necessary for efficient competition in mammals (Kimberlin and Walker, 1985;Bartz et al., 2007;Shikiya et al., 2010).As a direct test of this prediction, our studies demonstrate that the recessive [PSI + ] Weak variant effectively competes for soluble Sup35 protein when the titer of the normally dominant [PSI + ] Strong variant is reduced by treatment with GdnHCl (Figure 6).This advantage, however, is transient, as colonies formed from diploid strains resulting from the mating of the titrated [PSI + ] Strong haploid to [psi − ], [PSI + ] Weak , and [PSI + ] Strong haploids all have the [PSI + ] Strong phenotype (Supplementary Figure S4), indicating that the dominant variant can overcome this initial setback.
The invariant dominance of [PSI + ] Strong , even when titrated, that we observe differs from a previous report, in which [PSI + ] Weak emerged in approximately one third of the progeny of diploids  (Sharma and Liebman, 2012).While we have been unable to reproduce this result with either our own or the original yeast strains, we cannot rule out the possibility that the original [PSI + ] Weak variant has evolved over time.Nonetheless, our observations that the [PSI + ] Weak variant persists in these diploids (Figure 2) and is capable of incorporating soluble Sup35 (Figure 4) and being processed by Hsp104 (Figure 5) suggest that variant competition is an on-going process in cells containing variant mixtures.As such, it can be altered, leading to re-emergence of a recessive variant if more favorable conditions arise.
The co-existence of yeast prion variants in individual cells is consistent with the co-existence of PrP Sc variants in mammals, including in humans (Polymenidou et al., 2005;Collinge and Clarke, 2007;Cassard et al., 2020).Such mixtures are particularly relevant for the transmission of prions among species and during exposure to anti-prion therapeutics, two conditions in which variant switches are often observed (Bruce and Dickinson, 1987;Ghaemmaghami et al., 2009;Roberts et al., 2009;Li et al., 2010;Oelschlegel and Weissmann, 2013).Although it is unclear whether these new variants are a result of conformational "mutation" or whether they are selected from an existing mixture, the transition, at some point, must involve the co-existence of distinct variants and a change in their competitive advantage.Such dynamics are difficult to reconcile with a model based solely on the intrinsic conversion rates of the corresponding amyloid structures.Rather, insight into these transitions must consider the broader system in which the competition for soluble prion protein occurs.The protein quality control apparatus that senses and responds to proteotoxic stress is a particularly relevant component of this system, given its known impact on prion aggregate fragmentation in yeast (Chernoff et al., 1995;Song et al., 2005;Satpute-Krishnan et al., 2007;Higurashi et al., 2008;Sadlish et al., 2008;Tipton et al., 2008).Indeed, mutations in chaperone proteins have previously been reported to differentially impact prion variants (Astor et al., 2018;Yu and King, 2018).Thus, the sensitivity of prion variant competition to even transient changes in chaperone activity in yeast that we have observed here provides an expanded framework for addressing the seemingly expansive adaptability of prion variants in vivo.

Plasmid construction
All bacterial plasmids used in this study are listed in Table 2.All oligonucleotides are listed in Table 3.
SB869 was constructed from SB117 using QuikChangeII sitedirected mutagenesis kit (Agilent) with primers G20DSup35 F and G20DSup35 R. The mutation was confirmed by sequencing using G20D check.SB1047 was constructed by subcloning the tetracycline inducible promoter, P tetO7 , from SB661 into SB869 via restriction sites ClaI and BamHI.SB1120 was constructed by amplifying the coding sequence for methionine plus amino acids 11-61 from SB117 using primers F 11-61 BamHI and R 11-61 Xba1, followed by subcloning into SB105.The mCherry sequence was amplified from SB604 using primers XbaI mcherry F and SacI mcherry R and subcloned into SB101.SB1133 was constructed by amplifying GFP coding sequence from SB117 with primers F GFP XbaI and R GFP SacI.The amplified sequence was and subcloned into SB1120 via XbaI and SacI restriction sites.All restriction enzymes were obtained from New England BioLabs, Ipswitch, MA.

Strain construction
All yeast strains used in this study are derivatives of the 74-D694 strain (Chernoff et al., 1995) and are listed in Table 4.All oligonucleotides are listed in Table 3. SY3522, SY3523 and SY3524 were constructed by disrupting ADE1 in SLL3260, SY3619, and SLL3251, respectively, with a PCR-generated ADE1 knock-out cassette amplified from pFA6aKanMX4 (Longtine et al., 1998) using ADE13'KO and ADE15'KO.Strains were screened for ADE1 disruption by PCR of genomic DNA using primers Ade15'Ch and Ade13'Ch, sporulated and verified for 2:2 segregation of the appropriate marker and colony color phenotype.SY3619 was constructed by mating SLL2600 and SY3609; the latter strain was obtained via a mating-type switch of SLL2600.SY3260 was constructed by mating SLL2119 to SY3250.Construction of SY597 has been previously described (Satpute-Krishnan et al., 2007), and the corresponding [PSI + ] Weak strain, SY932 was constructed by integrating Eco47III-digested SB117 into SY1220.SY2201 and SY2203 were constructed by integrating Eco47IIIdigested SB869 in SLL2600 and SLL2606, respectively.SY3088 and SY3193 were constructed by integrating a PpuMI-digested SB1047 in SLL2119 and SLL2600, respectively.SY2393 and SY2686 were constructed by integrating a Bsu36I-digested SB910 in SLL3251 and SY1220, respectively.SY3421 and SY3423 were constructed by integrating Eco47III-digested SB1120 into SLL2600 and SLL2606, respectively.SY3446 was constructed by integration of Eco47IIIdigested SB1133 in SY2606.All strains expressing GFP and mCherry were screened for fluorescence by microscopy.

General growth conditions
All strains were grown in YPAD medium [2% dextrose Fisher Scientific, D16), 1% Bactopeptone (Gibco, 211,677), 1% yeast extract (Millipore, 1,037,530,500)] with 3 adenine (Sigma-Aldrich, A8626) unless otherwise specified.All overnight cultures were grown in a shaking incubator at 30°C and maintained at a growth of OD 600 less than 0.5 for at least 10 doublings to ensure that all experiments were conducted on cells undergoing exponential growth.

Crosses with Δade strains
Strains were cultured in liquid SC medium containing 15 mg/L adenine (Sigma-Aldrich, A8626) overnight and harvested in early log phase in the morning.Strains of opposite mating type were juxtaposed on SC solid medium for <30 min, mixed to commence mating, then transferred to SC solid medium with reduced adenine (5 mg/L).After ~4 h, patched mated mixtures were transferred to SC solid medium containing 2.5 mg/L adenine and 200 mg/L cytosine (Sigma-Aldrich, C3506) and a pre-embedded microscope slide.Individual zygotes were micromanipulated to the area over the microscope slide.Zygotes were incubated at 30°C in a humidified enclosure for 2 days before the slide was cut out for imaging.Microcolonies were inspected by microscopy, and the number of cells were counted.

Persistence of [PSI + ] Weak aggregates
Zygotes expressing Sup35(G20D)-GFP from P tetO7 were transferred to minimal medium containing 10 μg/mL doxycycline (Sigma-Aldrich, D9891) for 12 h.Zygotes were isolated by micromanipulation, and agar pads with zygotes were cut from plates and transferred to microscope slides for imaging.

Propagon counts
The number of propagons per cell/zygote was determined by an in vivo colony-based dilution assay, as previously described (Cox et al., 2003).Propagon variants (i.e., [PSI + ] Strong and [PSI + ] Weak ) were determined by their respective white and pink colony phenotypes and quantified.To assess effects of GdnHCl on propagon counts and to obtain the titrated [PSI + ] Strong strain, [PSI + ] Strong cultures were grown in liquid YPAD medium supplemented with 3 mM GdnHCl (Sigma-Aldrich).

Stop codon readthrough assay
Cultures were grown in liquid SC medium supplemented 2.5 mM adenine (Sigma-Aldrich, A8626) overnight, harvested and incubated in medium conditioned by cells of the opposite mating type for 1 h.In each cross, one mating partner expressed the GST(UGA)-YFP-NLS reporter from an integrated copy of the SB910 plasmid.Equal OD 600 units of each mating partner were then mixed and incubated on solid SC medium supplemented with 2.5 mM adenine and allowed to mate for 4 h at 30°C.Cells were then resuspended in liquid SC medium supplemented with 2.5 mM adenine and transferred to microscope slides for imaging.Readthrough activity was determined by measuring the fluorescence in zygotes from each cross versus the signal from a control mating between [psi − ] haploids expressing the reporter.The measured

Imaging
Imaging was performed in SC medium supplemented with 2.5 mM adenine.Images were obtained on a Zeiss AxioImager M2 with a 100x objective.Fluorescence intensity was analyzed using the Zen software package (Zeiss, Germany).Confocal images were acquired on Leica SP8X confocal microscope equipped with a 63x oil immersion objective and LASX software package.

Imaging and fluorescence loss in photobleaching
Experiments were performed on a Nikon TiE stand equipped with Yokogawa Spinning Disk confocal and FRAP/PA unit for perturbations, using NIS Elements software.Fluorescence Images were acquired with a 60X oil immersion objective, 4×4 bin, 488 nm excitation using 10-15% laser power with 1 and 100% transmission for image acquisitions and bleaching, respectively.Fifteen bleach-image iterations were performed for each zygote with bleaching duration of 2.5 s, laser dwell time of 1,000 us, and image acquisitions every 2 s.Mature daughter buds roughly 1/3-1/2 the size of the entire zygote, were chosen, and bleaching area was kept roughly the same for each zygote; zygotes were individually inspected prior to each FLIP acquisition to ensure septation of bud had not occurred.For each image frame, the average fluorescence pixel intensity was recorded in the mother cell, the bleached bud, a nearby reference cell, and the background.Time-lapse fluorescence intensities in the mother cells were normalized to background and reference levels according to published methods (Bolognesi et al., 2015).

Processing of FLIP measurements and estimating fluorescence loss rates
To extract biological information from the FLIP measurements (Bolognesi et al., 2015), we first adjust the raw intensity measurements for the mother cell [m raw (t)], using the background b raw and reference cell r raw intensities for each measurement time point t, as follows: 1 Background Correction: Subtract the background intensity from the mother and reference cell measurements, • Corrected mother cell intensity: m corrected (t) = m raw (t) -b raw (t) • Corrected reference cell intensity: r corrected (t) = r raw (t) -b raw (t) 2 Photobleaching Correction: Adjust for photobleaching by dividing the corrected mother measurements by the corrected reference intensity: • Adjusted mother cell intensity:m adjusted (t) = m corrected (t)/r corrected (t) 3 Normalization: Normalize the adjusted fluorescence intensity in the mother cell to show the fluorescence loss relative to the initial fluorescence measurement.This is done by dividing each adjusted fluorescence measurement made at time t i , by the initial fluorescence measurement made at time t 0 : • Normalized intensity: M(t i ) = m adjusted (t i )/ m adjusted (t 0 ).
After processing the FLIP measurements for each variant cross, we model the fluorescence loss in the mother relative to the initial fluorescence, M(t), as an exponential decay process.The fluorescence loss rate, denoted as λ (with units of per second), is estimated by fitting an exponential decay model exp.(-»t) to each replicate in each cross.This approach allows us to compare fluorescence loss rates between different variant crosses.

Statistical analyses of variant crosses 4.14.1 Fluorescence loss in photobleaching
For consistency and due to differences in the variance of the fluorescence loss estimates, we apply the unequal variance t-test when comparing the fluorescence loss between two conditions.This method is used even when there is no statistical evidence of differences in variance between the two groups (Ruxton, 2006).A p-value of less than 0.05 is significant statistical evidence of differences in the fluorescence loss between the two crosses being compared.

Propagon counts
When comparing three or more groups of propagon counts, we first perform an analysis of variance (ANOVA).Due to heteroskedasticity between variant crosses and deviations from normality, we utilize the more robust Welch's ANOVA test to determine if there are differences in mean propagon counts among the crossing being compared (Lantz, 2013).If the ANOVA indicates significant differences, we then conduct pairwise unequal variance t-tests for all variant crosses.To reduce type 1 errors (false positives) when comparing more than two groups, we indicate significance with an asterisk for those comparisons that remain significant after applying a Bonferroni correction to adjust our significance level of 0.05 (Nahler, 2009), while reporting all p-values.All computations, calibrations, and statistical analyses were performed using MATLAB R2023a (MathWorks, Inc., Natick, MA, USA).Specifically, model calibration we used the nlinfit function, and for the unequal variance t-test we used the ttest2 function with the 'vartype' option set to 'unequal' .

FIGURE 1
FIGURE 1 The [PSI + ] Strong phenotype is established immediately after variant mixing.(A) Δade1 [psi − ] (dark grey), Δade1 [PSI + ] Weak (light gray), and Δade1 [PSI + ] Strong (white) haploids were mated to wildtype (WT) [psi − ], [PSI + ] Weak , and [PSI + ] Strong haploids, and budding from the zygotes on synthetic complete medium was quantified.Results are presented as box-whisker plots.Horizontal lines indicate 25th, 50th, and 75th percentiles; whiskers indicate 10th and 90th percentiles; diamonds indicate means; outliers are presented as dots.The number of zygotes analyzed is presented in parentheses below each box plot.The equality of means across all groups was tested using Welch's ANOVA test (p* ANOVA ); p-values were determined using pairwise unequal variance t-tests and are presented above each box plot for comparisons within a cross.The absence of a p-value for comparisons within a cross indicates a lack of significant difference.Full statistical comparisons are available in Supplementary Table S1.(B) WT [psi − ], [PSI + ] Strong , and [PSI + ] Weak haploids were mated to a [PSI + ] Weak haploid expressing a fluorescent, nuclear localizing readthrough reporter, GST(UGA)-YFP-NLS.Representative epifluorescence images (eYFP) of the zygotes are shown alongside merged eYFP and Normarski images (DIC).(C) Fluorescence intensity within zygotes, representing stop codon readthrough levels, was quantified and presented in a box-whisker plot.Horizontal lines indicate 25th, 50th, and 75th percentiles; whiskers indicate 10th and 90th percentiles; diamonds indicate means; outliers are presented as dots.The number of zygotes analyzed is presented in parentheses below each box plot.The equality of means across all groups was tested using Welch's ANOVA test (p* ANOVA ); p-values were determined using pairwise unequal variance t-tests and are presented above each box plot for comparisons within a cross.The absence of a p-value for comparisons within a cross indicates a lack of significant difference.Full statistical comparisons are available in Supplementary TableS2.

FIGURE 2
FIGURE 2 The [PSI + ] Weak variant persists after mating to the dominant [PSI + ] Strong variant.(A) Wildtype (WT) [psi − ], [PSI + ] Weak , and [PSI + ] Strong haploids were mated to a WT [PSI + ] Strong haploid without treatment (untreated, dark gray), in the presence of 3 mM GdnHCl (treated, light gray), and in the presence of 3 mM GdnHCl following growth of the [PSI + ] Strong haploid (1N) in the presence of GdnHCl for 12 h (titrated, white).The number of [PSI + ] Strong propagons from the resulting zygotes and a [PSI + ] Strong haploid was quantified and presented as box-whisker plots.Horizontal lines indicate 25th, 50th, and 75th percentiles; whiskers indicate 10th and 90th percentiles; diamonds indicate means; outliers are presented as dots.The number of zygotes analyzed is presented in parentheses below each box plot.The equality of means across all groups was tested using Welch's ANOVA test (p* ANOVA ); p-values were determined using pairwise unequal variance t-tests and are presented above each box plot for comparisons within a cross.The absence of a p-value for comparisons within a cross indicates a lack of significant difference.Full statistical comparisons are available in Supplementary TableS3.(B) The number of [PSI + ] Weak propagons from the zygotes presented in (A) was quantified and presented as box-whisker plots as in (A).The equality of means across all groups was tested using Welch's ANOVA test (p* ANOVA ); p-values were determined using pairwise unequal variance t-tests and are presented above each box plot for comparisons within a cross.The absence of a p-value for comparisons within a cross indicates a lack of significant difference.Full statistical comparisons are available in Supplementary TableS4.(C) The persistence of the [PSI + ] Weak variant was observed by microscopy in crosses between [PSI + ] Strong and [PSI + ] Weak haploids expressing Sup35(G20D)-GFP under the control of the P tetO7 promoter.GFP foci were detected in cells at the periphery of the resulting microcolony, indicated by white arrows in the inset (200-fold magnification).
Although [PSI + ] Weak propagons are present in zygotes formed by mating a [PSI + ] Strong and a [PSI + ] Weak haploid (Figure 2B), they are not amplified to the diploid level (Figure 3, dark gray), perhaps suggesting a reduced rate of fragmentation during competition.To assess the fragmentation efficiency of aggregates of the [PSI + ] Weak variant in the presence or absence of aggregates of the [PSI + ] Strong

FIGURE 3
FIGURE 3 The dominant [PSI + ] Strong variant interferes with amplification of [PSI + ] Weak propagons.A wildtype (WT) [PSI + ] Weak haploid (1 N) was mated to WT [psi − ], [PSI + ] Weak , and [PSI + ] Strong haploids without treatment (untreated, dark gray) or in the presence of 3 mM GdnHCl (treated, white).The number of [PSI + ] Weak propagons from the zygotes and the [PSI + ] Weak haploid was quantified and presented in boxwhisker plots.Horizontal lines indicate 25th, 50th, and 75th percentiles; whiskers indicate 10th and 90th percentiles; diamonds indicate means.The number of zygotes analyzed is presented in parentheses below each box plot.The equality of means across all groups was tested using Welch's ANOVA test (p* ANOVA ); p-values were determined using pairwise unequal variance t-tests and are presented above each box plot for comparisons within a cross; the absence of a p-value for comparisons within a cross indicates a lack of significant.Full statistical comparisons are available in Supplementary TableS5.
, GFP foci remain visible(Satpute- Krishnan et al., 2007).If Sup35-GFP aggregates of the [PSI + ] Weak variant are poorly fragmented in the presence of the [PSI + ] Strong variant, we would expect the fluorescent foci to persist longer than in the absence of the competing prion.Upon mating a [PSI + ] Weak haploid expressing Sup35-GFP from P MFA1 to [psi − ], [PSI + ] Weak , or [PSI + ] Strong haploids, the resulting zygotes contain several GFP-labeled foci (Figure5A), and these complexes persist over several hours if fragmentation is inhibited with GdnHCl (Figure5A, right panel).In the absence of GdnHCl, fluorescent foci are no longer visible by 6 h in the zygotes formed by mating a [PSI + ] Weak haploid expressing Sup35-GFP from P MFA1 to [psi − ] and [PSI + ] Weak haploids, indicating that fragmentation of these aggregates is robust (Figure5B, right panel).Similarly, fluorescent foci are lost by 6 h in the absence of GdnHCl in zygotes formed by mating a [PSI + ] Weak haploid expressing Sup35-GFP from P MFA1 to a [PSI + ] Strong haploid, suggesting the presence of the [PSI + ] Strong variant does not substantially interfere with the fragmentation of Sup35 aggregates of the [PSI + ] Weak variant (Figure5B, right panel).Thus, prion variant competition is unlikely to arise through a modulation of fragmentation rate.

FIGURE 4
FIGURE 4 The dominant [PSI + ] Strong variant competes for soluble Sup35 more efficiently than the recessive [PSI + ] Weak variant.(A) Wildtype [PSI + ] Strong (blue) and [PSI + ] Weak haploids (salmon) were mated to a [PSI + ] Weak haploid expressing GFP-tagged Sup35 under the control of the P MFA1 promoter.Fluorescence intensity was quantified in the mother lobe of a singly budded zygote following repeated photobleaching of the daughter (left), and the rate of fluorescence loss was calculated and presented as box-whisker plots (right, n ≥ 11).Horizontal lines indicate 25th, 50th, and 75th percentiles; whiskers indicate 10th and 90th percentiles; diamonds indicate means.An unequal variance t-test was used to determine p values (B) A [PSI + ] Weak haploid expressing a GFP-tagged Sup35 mutant (G20D) under the control of the P MFA1 promoter was mated to wildtype [PSI + ] Strong (blue) and [PSI + ] Weak (salmon) haploids and analyzed as in (A, n ≥ 13).
) of the [PSI + ] Strong variant in the presence of the [PSI + ] Weak variant cannot be explained by its lower inherent rate of conversion, the relative sensitivity of the amplification of [PSI + ] Strong propagons to Hsp104 activity may suggest that template number is a key determinant of variant competition.To test this idea, we grew a [PSI + ] Strong haploid in the presence of GdnHCl for 12 h, hereafter referred to as titrated [PSI + ] Strong .This treatment leads to a reduction in [PSI + ] Strong propagons (Figure 6A) to a level below that of [PSI + ] Weak propagons in [PSI + ] Weak haploids (Figure 3) without curing [PSI + ] Strong .Consistent with the decrease in propagons, the titrated [PSI + ] Strong haploid has a corresponding increase in soluble Sup35, similar to the level found in a [psi − ] haploid (Supplementary Figure S3).To determine how the number of [PSI + ] Strong propagons affects competition, we mated the titrated [PSI + ] Strong haploid with [psi − ], [PSI + ] Strong , and [PSI + ] Weak haploids in the presence of GdnHCl.The amplification of [PSI + ] Strong propagons observed in zygotes formed by FIGURE 5Competing variants are differentially affected by fragmentation activity.(A,B) A [PSI + ] Weak haploid expressing GFP-tagged Sup35 under the control of the P MFA1 promoter was mated to the indicated wildtype haploids in the presence or absence of guanidine hydrochloride (+/-GdnHCl).For each cross, a representative zygote (left column) and its resulting microcolony (right column) are shown (n > 8).Note that the differences in fluorescent intensity between zygotes (+/-GdnHCl) are explained by the incorporation of soluble Sup35-GFP onto newly introduced prion aggregates that are or are not being fragmented, as expected(Satpute-Krishnan et al., 2007).

FIGURE 6
FIGURE 6 The competitive advantage of [PSI + ] Strong is limited by template abundance.(A) The number of [PSI + ] Strong propagons was determined at 3-h intervals in the presence of guanidine hydrochloride (GdnHCl) (n > 12).Results are presented as box-whisker plots.Horizontal lines indicate 25th, 50th, and 75th percentiles; whickers indicate 10th and 90th percentiles.(B) A [PSI + ] Strong haploid expressing GFP-tagged Sup35 under the control of the P MFA1 promoter was grown in the presence of GdnHCl for 12 h then mated to wildtype [PSI + ] Strong (blue) or [PSI + ] Weak haploids (salmon).The daughters of singly budded zygotes were subjected to repeated photobleaching while fluorescence intensity in the mother lobes was monitored (left) and the rates of fluorescence decay were calculated and presented as box-whisker plots (right, n ≥ 9).Horizontal lines indicate 25th, 50th, and 75th percentiles; whiskers indicate 10th and 90th percentiles.An unequal variance t-test was used to determine p-values.(C) A [PSI + ] Strong haploid expressing a GFPtagged Sup35 mutant (11-61) under the control of the P MFA1 promoter was grown in the presence of GdnHCl for 12 h and then crossed to wildtype [PSI + ] Strong (blue) and [PSI + ] Weak (salmon) haploids and analyzed as in (B, n ≥ 11).

TABLE 1
Fluorescence loss in photobleaching.
] Strong strain to a [PSI + ] Weak strain remains inhibited (Figure 2A, compare light gray to white).This observation suggests that [PSI + ] Weak can effectively interfere with the amplification of [PSI + ] Strong propagons when the propagon levels of the two variants are more balanced.Despite this inhibition of amplification of [PSI + ] Strong propagons, we also do not observe amplification of [PSI + ] Weak propagons, which accumulate to indistinguishable levels in the zygotes formed by mating a [PSI + ] Weak haploid to either a titrated [PSI + ] Strong or [PSI + ] Strong haploid in the presence of GdnHCl (Figure 2B, compare light gray to white).Because the amplification of [PSI + ] Strong propagons correlates with the conversion of Sup35 to the [PSI + ] Strong state (Figures PSI + ] Strong and [PSI + ] Weak haploids